Increased Expression of Toll-Like Receptors 2 and 4 in Renal Transplant Recipients that Develop Allograft Dysfunction: A Cohort Study

<strong>Background: </strong>The incidence of ischemic reperfusion injury (IRI) in early phase post-transplantation and activation of toll-like receptor (TLR-2) and TLR-4 remarkably impact the outcome of a renal allograft. <strong>Objective: </strong>To investigate whether th...

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Bibliographic Details
Main Authors: Morteza Hosseinzadeh, Mohsen Nafar, Pedram Ahmadpoor, Farshid Noorbakhsh, Mir Saeed Yekaninejad, Mohammad Hossein Niknam, Aliakbar Amirzargar
Format: Article
Language:English
Published: Shiraz University of Medical Sciences 2017-03-01
Series:Iranian Journal of Immunology
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Online Access:http://iji.sums.ac.ir/article_39286_9155557e5753adf15f78c908488a2326.pdf
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Summary:<strong>Background: </strong>The incidence of ischemic reperfusion injury (IRI) in early phase post-transplantation and activation of toll-like receptor (TLR-2) and TLR-4 remarkably impact the outcome of a renal allograft. <strong>Objective: </strong>To investigate whether the expression of TLRs in peripheral blood mononuclear cells (PBMCs) can predict the clinical outcome of kidney allografts. <strong>Methods:</strong> We obtained blood samples from 52 renal transplant patients before transplant, and 2, 90, and 180 days post-transplantation in order to analyze the surface expressions of TLR-2 and TLR-4 on peripheral blood monocytes. The expression patterns of TLR-2 and TLR-4 were compared between patients with graft dysfunction (GD) and those with well-functioning graft (WFG). <strong>Results: </strong>Significantly different mean dynamic changes in surface expression of TLR-2, according to percentage of TLR-2<sup>+</sup> cells, between (the GD and WFG) groups existed at most time-points before and after renal transplantation (p=0.007) with the exception of  day 2 post-transplantation. We observed significantly higher mean fluorescence intensities of TLR-2 and TLR-4 on CD14<sup>+ </sup>cells in the GD group compared to the WFG group. This finding was particularly observed 180 days post-transplantation (p=0.001). Based on TLR-2 and TLR-4 protein expression for each step, multiple logistic regression and ROC curve analysis revealed that an increase in CD14<sup>+</sup> TLR-2<sup>+</sup> monocytes within the 90 days  post-transplantaton was associated with increased risk of GD at 180 and 365 days post-transplantation  [odds ratio (OR)=1.27, p=0.005)]. <strong>Conclusion:</strong> Sequential monitoring of TLR-2 and TLR-4 expression patterns in peripheral blood monocytes appear to be prognostic and predictive biomarkers for early and late kidney allograft outcomes.
ISSN:1735-1383
1735-367X